PlainRecalls

2024 Recalls

6,210 recalls · Page 45 of 125

2024 Recall Year Insight

Federal agencies issued 6,210 product recalls indexed by PlainRecalls in calendar year 2024. That represents about 6.11% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 17.0 recalls per day across the FDA, CPSC, and NHTSA combined. Year-level views are the cleanest way to see macro patterns: volume spikes often correlate with new regulatory priorities (e.g., infant-sleep products after 2021, lithium-ion batteries after 2022), supply-chain contamination events, or changes in agency enforcement intensity, while quiet years can reflect either genuine product-safety improvements or reduced agency staffing and reporting lag. With 125 pages at 50 recalls each, browsing this year end-to-end gives a statistically representative sample of what the federal recall pipeline looked like in 2024.

On this page of 50 records, severity classification shows 2 critical, 48 moderate, and 0 lower-severity recalls. The page references 15 distinct recalling firms operating in 1 distinct product categories, with 49 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (50), which matters because each agency's recall authority, hazard framing, and remedy mechanism differ, an FDA food recall, a CPSC consumer-product recall, and a NHTSA vehicle recall are legally distinct instruments even when the underlying hazard language sounds similar. Reviewing the dominant agency for a given year is one of the fastest ways to understand where federal attention was concentrated.

Year-indexed browsing serves three practical purposes: historical research (tracking how a hazard class evolved over time), consumer action (finding whether a product purchased in 2024 was later recalled), and journalistic or regulatory context (understanding what the enforcement landscape looked like in a given period). Every record on this page links to a full detail view with the hazard, remedy, distribution, and agency-assigned recall number, always use that recall number to verify current status directly with the issuing agency before acting on time-sensitive remedies, because agencies amend, terminate, and expand recalls in the months and years after initial publication. Data on this page reflects federal agency public filings; the agency's live record remains authoritative for legal, medical, or safety decisions. Verify with FDA openFDA, CPSC, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Moderate Aug 28, 2024

Product Desc: Product Name: A-OK SATINSLIT FULL HANDLE2.75MM ANG SG Model/Catalog Number: 8065992761 Software Version: N/A Product Description: Op…

Alcon Research LLC

FDA Devices Moderate Aug 28, 2024

Product Name: TOTAL PLUS,25+,10K VALVE WD Model/Catalog Number: 8065752438 Software Version: N/A Component: N/A

Alcon Research LLC

FDA Devices Moderate Aug 28, 2024

Medline medical procedure kits labeled as follows: a) BASIC NASAL, REF DYNJ909932; b) BRONCH KIT, REF DYKE1007B; c) ENT, REF DYNJ909935; d…

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Aug 28, 2024

Philips Allura Xper systems (R8.1 with Poly-G Stand) Interventional Fluoroscopic X-Ray System, Model Numbers 722010, 722012, 722013

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Aug 28, 2024

Product Name: 25GA VALVED ENTRY SYSTEM,3CT Model/Catalog Number: 8065751658 Software Version: N/A Product Description: Valved Trocar Entry System …

Alcon Research LLC

FDA Devices Moderate Aug 28, 2024

Product Name: 25+TTLPL VPK 20000CPM BEV VAL Model/Catalog Number: 8065753106 Software Version: N/A Component: N/A

Alcon Research LLC

FDA Devices Moderate Aug 28, 2024

1,5L MED-SOFT SINGLE LINER WITH SOLIDIFIER, REF OR1920PG

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Aug 28, 2024

Product Name: 25+ CMB PAK 10K CPM,V,WA 0.9 Model/Catalog Number: 8065752451 Software Version: N/A Component: N/A

Alcon Research LLC

FDA Devices Moderate Aug 28, 2024

Product Name: Alcon Custom Pak Model/Catalog Number: Many Software Version: N/A Product Description: Alcon Custom Paks are customer-designed steri…

Alcon Research LLC

FDA Devices Moderate Aug 28, 2024

Product Name: ClearCut S Safety Sideport Knife 1.0mm Dual Bevel Model/Catalog Number: 8065771540 Software Version: N/A Product Description: Ophtha…

Alcon Research LLC

FDA Devices Critical Aug 28, 2024

ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever Thrombectomy System, Reference: IU-…

Inari Medical - Oak Canyon

FDA Devices Moderate Aug 28, 2024

Multiple Digital Analog Products labeled as: NobelBiocare Tri-Lobe-compatible 6.0mm Digital Analog, REF 9000703 Straumann Tissue-Level-compatible W…

Preat Corp

FDA Devices Moderate Aug 28, 2024

Medline medical procedure kits labeled as follows: a) AAA CDS, REF CDS984011C; b) CAN KIT, REF DYKM1184; c) DENTAL CDS, REF CDS984010B; d) E…

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Aug 28, 2024

BIOFIRE FILMARRAY Pneumonia Panel, REF: RFIT-ASY-0144

BioFire Diagnostics, LLC

FDA Devices Moderate Aug 28, 2024

Vial Decanter, REF 2006S. Packaged on a form, fill and seal machine with a poly/Tyvek material then placed 50 products to a case (cs).

Microtek Medical Inc.

FDA Devices Moderate Aug 28, 2024

Medline medical procedure kits labeled as follows: a) TURNOVER KIT, REF DYKC1289F

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Aug 28, 2024

BD BACTEC MGIT 960 PZA Kit)- IVD qualitative procedure for susceptibility testing of Mycobacterium tuberculosis, from culture to pyrazinamide (PZA) …

Becton Dickinson & Co.

FDA Devices Moderate Aug 28, 2024

Spectrum Wireless Battery Modules A/B/G/N, product code 36010, used with either of the following 35700BAX2 (Spectrum V8 infusion pump) and 3570009 (S…

Baxter Healthcare Corporation

FDA Devices Moderate Aug 28, 2024

Covideien McGRATH MAC Video Laryngoscope, REF: 301-000-000, Non-Sterile, RxOnly

Covidien

FDA Devices Moderate Aug 28, 2024

Product Desc: Product Name: CLEARCUT SATINSLIT FULL HANDLE3.0MM ANG Model/Catalog Number: 8065993045 Software Version: N/A Product Description: Op…

Alcon Research LLC

FDA Devices Moderate Aug 28, 2024

IBA Proton Therapy System - PROTEUS 235- Designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other …

Ion Beam Applications S.A.

FDA Devices Moderate Aug 28, 2024

Product Name: 25+ TOTALPLUSr CP PAK 20K CPM BWV .9 IU Model/Catalog Number: 8065000093 Software Version: N/A Component: N/A

Alcon Research LLC

FDA Devices Moderate Aug 28, 2024

Product Name: 25+ CMB PAK 10K CPM,V,STD 0.9 Model/Catalog Number: 8065752450 Software Version: N/A Component: N/A

Alcon Research LLC

FDA Devices Moderate Aug 28, 2024

1,5L MED-SOFT LINER W/ 6MMX1,8M TUB. & ADULT VC, REF OR53926

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Aug 28, 2024

Baxter Spectrum Wireless Battery Modules A/B/G/N, product code 35223, used with either of the following: 35700BAX2 (Spectrum V8 infusion pump) or 35…

Baxter Healthcare Corporation

FDA Devices Moderate Aug 28, 2024

Regard Kit containing the Microtek decanter

ROi CPS LLC

FDA Devices Moderate Aug 28, 2024

Medline medical procedure kits labeled as follows: a) KIT CANISTER SUCT W 12FT, REF DYKM2169

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Aug 28, 2024

Medline medical procedure kits labeled as follows: DENTAL, REF DYNJ909211A

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Aug 28, 2024

The VITROS XT Chemistry Products ALB-TP Slides is a single device that contains both an albumin test and a total protein test side by side separated …

Ortho-Clinical Diagnostics, Inc.

FDA Devices Moderate Aug 28, 2024

1500ML SOFT LINER, 1/4X6 TBG NS, REF OR926K

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Aug 28, 2024

Medline medical procedure kits labeled as follows: a) ENDO KIT, REF DYKE1410A

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Aug 28, 2024

Medline medical procedure kits labeled as follows: a) BASIC NEURO, REF DYNJ909171A; b) NEURO, REF DYNJ905510D; c) NEURO, REF DYNJ902388L; d)…

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Aug 28, 2024

Product Desc: Product Name: ClearCut Sideport Knife Dual Bevel 1.2mm Angled Model/Catalog Number: 8065921541 Software Version: N/A Product Descrip…

Alcon Research LLC

FDA Devices Critical Aug 28, 2024

McGRATH" MAC EMS Video Laryngoscope, REF: 300-200-000 , Non-Sterile, Rx Only

Covidien

FDA Devices Moderate Aug 28, 2024

Product Name: 25+ TOTALPLUS CP PAK 20K CPM BV .9 IU Model/Catalog Number: 8065000095 Software Version: N/A Component: N/A

Alcon Research LLC

FDA Devices Moderate Aug 28, 2024

Product Name: TOTAL PLUS,25+,10K VALVE STD Model/Catalog Number: 8065752437 Software Version: N/A Component: N/A

Alcon Research LLC

FDA Devices Moderate Aug 28, 2024

Medline medical procedure kits labeled as follows: a) ANESTHESIA CIRCUIT ADULT, REF DYNJAAF6666B; b) ANESTHESIA CIRCUIT PEDS-LF, REF DYNJAP9918A…

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Aug 28, 2024

Medline medical procedure kits labeled as follows: a) GYN CDS, REF DYNJ905499B; b) GYN LAP, REF DYNJ909936; c) GYN LAPAROSCOPY, REF DYNJ902371…

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Aug 28, 2024

Product Name: 25+ CMB PAK 7.5CPM,V,STD 0.9 Model/Catalog Number: 8065751767 Software Version: N/A Component: N/A

Alcon Research LLC

FDA Devices Moderate Aug 28, 2024

Product Desc: Product Name: CLEARCUT SAFETY INTREPID SB,2.4 Model/Catalog Number: 8065772445 Software Version: N/A Product Description: Ophthalmic…

Alcon Research LLC

FDA Devices Moderate Aug 28, 2024

1,5L MED-SOFT LINER W/ 6MMX3M TUB. & ADULT VC, REF OR53929

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Aug 28, 2024

Product Desc: Product Name: CLEARCUT SAFETY INTREPID SB,2.2 Model/Catalog Number: 8065772245 Software Version: N/A Product Description: Ophthalmic…

Alcon Research LLC

FDA Devices Moderate Aug 28, 2024

Product Desc: Product Name: CLEARCUT SAFETY INTREPID DB,2.4 Model/Catalog Number: 8065772465 Software Version: N/A Product Description: Ophthalmic…

Alcon Research LLC

FDA Devices Moderate Aug 28, 2024

Product Desc: Product Name: CLEARCUT SAFETY INTREPID DB,2.2 Model/Catalog Number: 8065772265 Software Version: N/A Product Description: Ophthalmic…

Alcon Research LLC

FDA Devices Moderate Aug 28, 2024

Bottle Decanter, REF 2004S. Packaged on a form, fill and seal machine with a poly/Tyvek material then placed 50 products to a case (cs).

Microtek Medical Inc.

FDA Devices Moderate Aug 28, 2024

Ventana anti-CD10 (SP67) Rabbit Monoclonal Primary Antibody, REF: 790-4506, IVD

Ventana Medical Systems, Inc.

FDA Devices Moderate Aug 28, 2024

Medline medical procedure kits labeled as follows: a) ENDO KIT, REF DYK1012268E1

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Aug 28, 2024

Product Name: 25+ TTL PLUS VPAK 20000CPM BWV Model/Catalog Number: 8065830077 Software Version: N/A Product Description: Standardized assemblage o…

Alcon Research LLC

FDA Devices Moderate Aug 28, 2024

GM60A. Digital Diagnostic Mobile X-Ray System.

NeuroLogica Corporation

FDA Devices Moderate Aug 28, 2024

Product Desc: Product Name: CLEARCUT SATINSLIT FULL HANDLE2.75MM AN Model/Catalog Number: 8065992745 Software Version: N/A Product Description: Op…

Alcon Research LLC

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2024 with 2023 →

Data Sources

  • Source: FDA openFDA Enforcement API - calendar-year recall filings for food, drugs, and devices
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2024

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Figures cover calendar year 2024 across the FDA, CPSC and NHTSA federal recall feeds. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.